Please use this identifier to cite or link to this item: https://elar.urfu.ru/handle/10995/90046
Title: Synthesis of Heteroannulated Indolopyrazines through Domino N-H Palladium-Catalyzed/Metal-Free Oxidative C-H Bond Activation
Authors: Kvashnin, Y. A.
Verbitskiy, E. V.
Zhilina, E. F.
Rusinov, G. L.
Chupakhin, O. N.
Charushin, V. N.
Issue Date: 2020
Publisher: American Chemical Society
Citation: Synthesis of Heteroannulated Indolopyrazines through Domino N-H Palladium-Catalyzed/Metal-Free Oxidative C-H Bond Activation / Y. A. Kvashnin, E. V. Verbitskiy, E. F. Zhilina, G. L. Rusinov, et al. . — DOI 10.1021/acsomega.0c01945 // ACS Omega. — 2020. — Vol. 25. — Iss. 5. — P. 15681-15690.
Abstract: A convenient approach to [1,2,5]oxadiazolo[3′,4′:5,6]pyrazino[2,3-b]indoles and their heteroannulated analogues bearing various aryl substituents in the backbone has been developed. This synthetic protocol is based on Pd-catalyzed Buchwald-Hartwig and subsequent annulation by intramolecular oxidative cyclodehydrogenation. The photophysical properties for new polycycles have been measured. © 2020 American Chemical Society.
URI: http://elar.urfu.ru/handle/10995/90046
Access: info:eu-repo/semantics/openAccess
SCOPUS ID: 85087745933
WOS ID: 000546100300086
PURE ID: 13401406
ISSN: 2470-1343
DOI: 10.1021/acsomega.0c01945
Sponsorship: Russian Foundation for Basic Research, RFBR: 18-29-23045, 18-33-00103-mol_a
This work was supported by the Russian Foundation for Basic Research (research project no. 18-29-23045 mk). Y.A.K. would like to acknowledge the financial support for the part of the synthetic section from the Russian Foundation for Basic Research (research project no. 18-33-00103-mol_a).
Appears in Collections:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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